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Results of Tc99m-Maraciclatide Scintigraphy in Subjects With Diabetes Mellitus and Heart Failure With Preserved Left Ventricular Ejection Fraction

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General Electric (GE)

Status and phase

Terminated
Phase 2

Conditions

Diabetes Mellitus
Heart Failure

Treatments

Drug: Tc99m-Maraciclatide

Study type

Interventional

Funder types

Industry

Identifiers

NCT01440517
GE-078-101

Details and patient eligibility

About

The purpose of this study is to evaluate the results of 99mTc maraciclatide scintigraphy in diabetic subjects with HFPEF. A maximum of 20 subjects with Diabetes Mellitus (DM) and Heart Failure With Preserved Left Ventricular Ejection Fraction (HFPEF) will be enrolled and imaged with 99mTc maraciclatide. In addition, a maximum of 10 subjects with DM and diastolic dysfunction but no diagnosis of heart failure (HF) will be enrolled and imaged with 99mTc-maraciclatide.

Enrollment

4 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The subject is between 18 and 80 years of age.
  • The subject was diagnosed with DM type 2 based upon accepted clinical criteria and currently takes at least one diabetes medication.
  • For HF subjects: The subject was diagnosed with HF with preserved EF within the previous 1 year, at which time LVEF was determined to be ≥45%.
  • For comparison subjects: The subject was determined to have diastolic dysfunction on EKG within the previous year and currently has no signs or symptoms of HF.
  • The subject has been clinically stable for at least 7 days prior to the study imaging procedures (e.g., not experiencing continuing chest pain, hemodynamic instability, worsening HF symptoms, or clinically significant arrhythmia).

Exclusion criteria

  • The subject had an acute myocardial infarction within the past 30 days.
  • The subject had a cardiac revascularization (e.g., percutaneous transluminal coronary angiography [PTCA], percutaneous coronary intervention (PCI), or coronary artery bypass graft [CABG]) within the past 30 days.
  • The subject has severe renal dysfunction.
  • The subject is claustrophobic or has a movement disorder that prevents him/her from lying still in a supine position for up to 20 minutes at a time.
  • The subject has participated in a research study using ionizing radiation in the previous 12 months.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

4 participants in 1 patient group

Tc99m-Maraciclatide
Experimental group
Treatment:
Drug: Tc99m-Maraciclatide

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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